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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550371Generated: October 30, 2026

Triethylamine → N-(5-Fluoropyridin-2-yl)pivalamide

https://huagongshe.com/reaction/550371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPivaloyl chlorideHCID 62493—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Amino-5-fluoropyridineHCID 2737701—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductN-(5-Fluoropyridin-2-yl)pivalamideHCID 2229323776.6%

Reaction Steps

To a 0° C. solution of 2-amino-5-fluoropyridine (1.00 g, 8.92 mmol) and triethylamine (1.35 g, 13.4 mmol) in dichloromethane (30 mL) was added trimethylacetyl chloride (1.29 g, 10.7 mmol) and DMAP (0.11 g, 0.89 mmol). The solution was allowed to warm to room temperature. After 4 h, saturated aqueous NaHCO3 was added, the layers separated and the aqueous phase backwashed with DCM. The combined organics were dried over magnesium sulfate, filtered and concentrated and the residue purified by silica gel chromatography (5%→40% EtOAc/hexanes) to give the title compound (1.34 g). MS: m/z=197.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947678B2
Source datasetuspto-grants-2011_05
ORD IDord-abd55c44b76f4cfe881496d1d95226aa
Source noteuspto-grants-2011_05